CN106715395B - 作为taar调节剂的6-氨基-5,6,7,8-四氢萘-2-基或3-氨基色满-7-基衍生物 - Google Patents
作为taar调节剂的6-氨基-5,6,7,8-四氢萘-2-基或3-氨基色满-7-基衍生物 Download PDFInfo
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- CN106715395B CN106715395B CN201580035425.9A CN201580035425A CN106715395B CN 106715395 B CN106715395 B CN 106715395B CN 201580035425 A CN201580035425 A CN 201580035425A CN 106715395 B CN106715395 B CN 106715395B
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- amino
- tetrahydronaphthalen
- carboxamide
- tetrahydronaphthalene
- trifluoromethyl
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- -1 6-amino-5, 6, 7, 8-tetrahydronaphthalen-2-yl Chemical class 0.000 title claims description 72
- 108050002178 Trace amine associated receptor Proteins 0.000 title description 13
- 102000011829 Trace amine associated receptor Human genes 0.000 title description 11
- 150000001875 compounds Chemical class 0.000 claims abstract description 141
- 208000008589 Obesity Diseases 0.000 claims abstract description 25
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 20
- 208000035475 disorder Diseases 0.000 claims abstract description 19
- 150000003839 salts Chemical class 0.000 claims abstract description 18
- 239000002253 acid Substances 0.000 claims abstract description 16
- 208000030814 Eating disease Diseases 0.000 claims abstract description 8
- 208000019454 Feeding and Eating disease Diseases 0.000 claims abstract description 8
- 208000019695 Migraine disease Diseases 0.000 claims abstract description 8
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- 208000006096 Attention Deficit Disorder with Hyperactivity Diseases 0.000 claims abstract description 7
- 206010012601 diabetes mellitus Diseases 0.000 claims abstract description 7
- 235000020824 obesity Nutrition 0.000 claims abstract description 7
- 208000028017 Psychotic disease Diseases 0.000 claims abstract description 6
- 208000030159 metabolic disease Diseases 0.000 claims abstract description 6
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- 238000000034 method Methods 0.000 claims description 22
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- 125000000217 alkyl group Chemical group 0.000 claims description 11
- 229910052736 halogen Inorganic materials 0.000 claims description 11
- 239000001257 hydrogen Substances 0.000 claims description 11
- 229910052739 hydrogen Inorganic materials 0.000 claims description 11
- 150000002367 halogens Chemical class 0.000 claims description 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
- 125000005843 halogen group Chemical group 0.000 claims description 7
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- NDAXSCLCJGFDLB-UHFFFAOYSA-N N-(6-amino-5,6,7,8-tetrahydronaphthalen-2-yl)-2-(trifluoromethyl)pyridine-4-carboxamide Chemical compound NC1CC=2C=CC(=CC=2CC1)NC(C1=CC(=NC=C1)C(F)(F)F)=O NDAXSCLCJGFDLB-UHFFFAOYSA-N 0.000 claims description 4
- HSTSJLQWWRNUQR-CQSZACIVSA-N N-[(6R)-6-amino-5,6,7,8-tetrahydronaphthalen-2-yl]-1-(2,2-difluoroethyl)-5-propylpyrazole-3-carboxamide Chemical compound N[C@H]1CC=2C=CC(=CC=2CC1)NC(=O)C1=NN(C(=C1)CCC)CC(F)F HSTSJLQWWRNUQR-CQSZACIVSA-N 0.000 claims description 4
- IGDCSHQTDPJRSJ-LBPRGKRZSA-N N-[(6S)-6-amino-5,6,7,8-tetrahydronaphthalen-2-yl]-4-bromo-5-(2,2-difluoroethoxy)-1-ethylpyrazole-3-carboxamide Chemical compound N[C@@H]1CC=2C=CC(=CC=2CC1)NC(=O)C1=NN(C(=C1Br)OCC(F)F)CC IGDCSHQTDPJRSJ-LBPRGKRZSA-N 0.000 claims description 4
- YCCHXWKBRXFQKX-AWEZNQCLSA-N (6S)-6-amino-N-[3-(trifluoromethoxy)phenyl]-5,6,7,8-tetrahydronaphthalene-2-carboxamide Chemical compound N[C@@H]1CC=2C=CC(=CC=2CC1)C(=O)NC1=CC(=CC=C1)OC(F)(F)F YCCHXWKBRXFQKX-AWEZNQCLSA-N 0.000 claims description 3
- QCIDIKFLFHFGGC-AWEZNQCLSA-N 1-[(6S)-6-amino-5,6,7,8-tetrahydronaphthalen-2-yl]-3-(4-chlorophenyl)urea Chemical compound N[C@@H]1CC=2C=CC(=CC=2CC1)NC(=O)NC1=CC=C(C=C1)Cl QCIDIKFLFHFGGC-AWEZNQCLSA-N 0.000 claims description 3
- AKWIAIDKXNKXDI-UHFFFAOYSA-N 1h-pyrrole-3-carboxamide Chemical class NC(=O)C=1C=CNC=1 AKWIAIDKXNKXDI-UHFFFAOYSA-N 0.000 claims description 3
- ZVPANFDUERACPH-GFCCVEGCSA-N COC1=CC(NC2=CC=C3C[C@@H](N)COC3=C2)=CC=C1 Chemical compound COC1=CC(NC2=CC=C3C[C@@H](N)COC3=C2)=CC=C1 ZVPANFDUERACPH-GFCCVEGCSA-N 0.000 claims description 3
- HSTSJLQWWRNUQR-UHFFFAOYSA-N N-(6-amino-5,6,7,8-tetrahydronaphthalen-2-yl)-1-(2,2-difluoroethyl)-5-propylpyrazole-3-carboxamide Chemical compound NC1CC=2C=CC(=CC=2CC1)NC(=O)C1=NN(C(=C1)CCC)CC(F)F HSTSJLQWWRNUQR-UHFFFAOYSA-N 0.000 claims description 3
- ZIXMJUDJEHWBIY-LLVKDONJSA-N N-[(3R)-3-amino-3,4-dihydro-2H-chromen-7-yl]-2-(trifluoromethyl)pyridine-4-carboxamide Chemical compound N[C@H]1COC2=CC(=CC=C2C1)NC(C1=CC(=NC=C1)C(F)(F)F)=O ZIXMJUDJEHWBIY-LLVKDONJSA-N 0.000 claims description 3
- SAPXEMBMLFBZPH-GFCCVEGCSA-N N-[(3R)-3-amino-3,4-dihydro-2H-chromen-7-yl]-2-chloro-6-methylpyridine-4-carboxamide Chemical compound N[C@H]1COC2=CC(=CC=C2C1)NC(C1=CC(=NC(=C1)C)Cl)=O SAPXEMBMLFBZPH-GFCCVEGCSA-N 0.000 claims description 3
- ZNDPFPKYIDQXPG-MRXNPFEDSA-N N-[(3R)-3-amino-3,4-dihydro-2H-chromen-7-yl]-4-(2-methyl-1,3-thiazol-4-yl)benzamide Chemical compound N[C@H]1COC2=CC(=CC=C2C1)NC(C1=CC=C(C=C1)C=1N=C(SC=1)C)=O ZNDPFPKYIDQXPG-MRXNPFEDSA-N 0.000 claims description 3
- LMPDYTWESHDVQA-SNVBAGLBSA-N N-[(3R)-3-amino-3,4-dihydro-2H-chromen-7-yl]-4-bromo-5-(2,2-difluoroethoxy)-1-ethylpyrazole-3-carboxamide Chemical compound N[C@H]1COC2=CC(=CC=C2C1)NC(=O)C1=NN(C(=C1Br)OCC(F)F)CC LMPDYTWESHDVQA-SNVBAGLBSA-N 0.000 claims description 3
- FTMLZGKFCRGKLY-SECBINFHSA-N N-[(3R)-3-amino-3,4-dihydro-2H-chromen-7-yl]-4-chloropyrimidine-2-carboxamide Chemical compound N[C@H]1COC2=CC(=CC=C2C1)NC(=O)C1=NC=CC(=N1)Cl FTMLZGKFCRGKLY-SECBINFHSA-N 0.000 claims description 3
- NCFYLVIYDDRAQM-SNVBAGLBSA-N N-[(3R)-3-amino-3,4-dihydro-2H-chromen-7-yl]-5-(trifluoromethyl)pyrimidine-2-carboxamide Chemical compound N[C@H]1COC2=CC(=CC=C2C1)NC(=O)C1=NC=C(C=N1)C(F)(F)F NCFYLVIYDDRAQM-SNVBAGLBSA-N 0.000 claims description 3
- MFDMZDJAISZKRR-LBPRGKRZSA-N N-[(3S)-3-amino-3,4-dihydro-2H-chromen-7-yl]-1-(2,2-difluoroethyl)-5-propylpyrazole-3-carboxamide Chemical compound N[C@@H]1COC2=CC(=CC=C2C1)NC(=O)C1=NN(C(=C1)CCC)CC(F)F MFDMZDJAISZKRR-LBPRGKRZSA-N 0.000 claims description 3
- DIRQXYSZUVPSOU-GFCCVEGCSA-N N-[(6R)-6-amino-5,6,7,8-tetrahydronaphthalen-2-yl]-6-methyl-2-(trifluoromethyl)pyrimidine-4-carboxamide Chemical compound N[C@H]1CC=2C=CC(=CC=2CC1)NC(=O)C1=NC(=NC(=C1)C)C(F)(F)F DIRQXYSZUVPSOU-GFCCVEGCSA-N 0.000 claims description 3
- HSTSJLQWWRNUQR-AWEZNQCLSA-N N-[(6S)-6-amino-5,6,7,8-tetrahydronaphthalen-2-yl]-1-(2,2-difluoroethyl)-5-propylpyrazole-3-carboxamide Chemical compound N[C@@H]1CC=2C=CC(=CC=2CC1)NC(=O)C1=NN(C(=C1)CCC)CC(F)F HSTSJLQWWRNUQR-AWEZNQCLSA-N 0.000 claims description 3
- LWDNGARBBRDLEK-HNNXBMFYSA-N N-[(6S)-6-amino-5,6,7,8-tetrahydronaphthalen-2-yl]-1-(3,4-dichlorophenyl)pyrazole-4-carboxamide Chemical compound N[C@@H]1CC=2C=CC(=CC=2CC1)NC(=O)C=1C=NN(C=1)C1=CC(=C(C=C1)Cl)Cl LWDNGARBBRDLEK-HNNXBMFYSA-N 0.000 claims description 3
- QPSSPMVEJOYPRO-SFHVURJKSA-N N-[(6S)-6-amino-5,6,7,8-tetrahydronaphthalen-2-yl]-1-(4-methylphenyl)pyrazole-4-carboxamide Chemical compound N[C@@H]1CC=2C=CC(=CC=2CC1)NC(=O)C=1C=NN(C=1)C1=CC=C(C=C1)C QPSSPMVEJOYPRO-SFHVURJKSA-N 0.000 claims description 3
- NDAXSCLCJGFDLB-ZDUSSCGKSA-N N-[(6S)-6-amino-5,6,7,8-tetrahydronaphthalen-2-yl]-2-(trifluoromethyl)pyridine-4-carboxamide Chemical compound N[C@@H]1CC=2C=CC(=CC=2CC1)NC(C1=CC(=NC=C1)C(F)(F)F)=O NDAXSCLCJGFDLB-ZDUSSCGKSA-N 0.000 claims description 3
- DIRQXYSZUVPSOU-LBPRGKRZSA-N N[C@@H]1CC=2C=CC(=CC=2CC1)NC(=O)C1=NC(=NC(=C1)C)C(F)(F)F Chemical compound N[C@@H]1CC=2C=CC(=CC=2CC1)NC(=O)C1=NC(=NC(=C1)C)C(F)(F)F DIRQXYSZUVPSOU-LBPRGKRZSA-N 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 230000008569 process Effects 0.000 claims description 3
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 3
- 238000006467 substitution reaction Methods 0.000 claims description 3
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 3
- XCUAIINAJCDIPM-XVFCMESISA-N N(4)-hydroxycytidine Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=NO)C=C1 XCUAIINAJCDIPM-XVFCMESISA-N 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 125000002541 furyl group Chemical class 0.000 claims description 2
- 125000001072 heteroaryl group Chemical group 0.000 claims description 2
- 125000001624 naphthyl group Chemical group 0.000 claims description 2
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 2
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 2
- 125000004076 pyridyl group Chemical group 0.000 claims description 2
- 125000000335 thiazolyl group Chemical class 0.000 claims description 2
- 125000001544 thienyl group Chemical class 0.000 claims description 2
- 238000011321 prophylaxis Methods 0.000 claims 3
- 230000001225 therapeutic effect Effects 0.000 claims 3
- IATSCFYTCJGHQI-ILSZIBLNSA-N (2S)-6-N-(5-chloropyrimidin-2-yl)-1,2,3,4-tetrahydronaphthalene-2,6-diamine (2S)-6-N-[5-(trifluoromethyl)pyrimidin-2-yl]-1,2,3,4-tetrahydronaphthalene-2,6-diamine Chemical compound ClC=1C=NC(=NC1)NC=1C=C2CC[C@@H](CC2=CC1)N.FC(C=1C=NC(=NC1)NC=1C=C2CC[C@@H](CC2=CC1)N)(F)F IATSCFYTCJGHQI-ILSZIBLNSA-N 0.000 claims 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 1
- PEDGHYLGBFMOFC-HQUXEWOTSA-N 1-[(6S)-6-amino-5,6,7,8-tetrahydronaphthalen-2-yl]-3-(4-ethylphenyl)urea 1-[(6S)-6-amino-5,6,7,8-tetrahydronaphthalen-2-yl]-3-[4-(trifluoromethoxy)phenyl]urea Chemical compound N[C@@H]1CC=2C=CC(=CC2CC1)NC(=O)NC1=CC=C(C=C1)OC(F)(F)F.N[C@@H]1CC=2C=CC(=CC2CC1)NC(=O)NC1=CC=C(C=C1)CC PEDGHYLGBFMOFC-HQUXEWOTSA-N 0.000 claims 1
- OWXORUFFMAJVEF-WMISSQJSSA-N 1-[(6S)-6-amino-5,6,7,8-tetrahydronaphthalen-2-yl]-3-[(5-chloropyridin-2-yl)methyl]urea 1-[(6S)-6-amino-5,6,7,8-tetrahydronaphthalen-2-yl]-3-[[3-(trifluoromethoxy)phenyl]methyl]urea Chemical compound N[C@@H]1CC=2C=CC(=CC2CC1)NC(=O)NCC1=CC(=CC=C1)OC(F)(F)F.N[C@@H]1CC=2C=CC(=CC2CC1)NC(=O)NCC1=NC=C(C=C1)Cl OWXORUFFMAJVEF-WMISSQJSSA-N 0.000 claims 1
- TWWVKJAXNGHMMP-UFRHTXTISA-N 1-[(6S)-6-amino-5,6,7,8-tetrahydronaphthalen-2-yl]-3-[4-(trifluoromethyl)phenyl]urea 1-[(6S)-6-amino-5,6,7,8-tetrahydronaphthalen-2-yl]-3-[6-(trifluoromethyl)pyridin-3-yl]urea Chemical compound N[C@@H]1CC=2C=CC(=CC2CC1)NC(=O)NC1=CC=C(C=C1)C(F)(F)F.N[C@@H]1CC=2C=CC(=CC2CC1)NC(=O)NC=1C=NC(=CC1)C(F)(F)F TWWVKJAXNGHMMP-UFRHTXTISA-N 0.000 claims 1
- LPACTABHZPNRKW-PFEQFJNWSA-N 6-amino-N-(4-cyanophenyl)-5,6,7,8-tetrahydronaphthalene-2-carboxamide (6R)-6-amino-N-[3-(trifluoromethoxy)phenyl]-5,6,7,8-tetrahydronaphthalene-2-carboxamide Chemical compound N[C@H]1CC=2C=CC(=CC2CC1)C(=O)NC1=CC(=CC=C1)OC(F)(F)F.NC1CC=2C=CC(=CC2CC1)C(=O)NC1=CC=C(C=C1)C#N LPACTABHZPNRKW-PFEQFJNWSA-N 0.000 claims 1
- NPEOADLXNMXICC-UHFFFAOYSA-N 6-amino-N-(4-ethylphenyl)-5,6,7,8-tetrahydronaphthalene-2-carboxamide 6-amino-N-[3-(trifluoromethoxy)phenyl]-5,6,7,8-tetrahydronaphthalene-2-carboxamide Chemical compound CCc1ccc(NC(=O)c2ccc3CC(N)CCc3c2)cc1.NC1CCc2cc(ccc2C1)C(=O)Nc1cccc(OC(F)(F)F)c1 NPEOADLXNMXICC-UHFFFAOYSA-N 0.000 claims 1
- VFRZKDPREVZOHV-UHFFFAOYSA-N 6-amino-N-[4-(trifluoromethyl)phenyl]-5,6,7,8-tetrahydronaphthalene-2-carboxamide 6-amino-N-[5-(trifluoromethyl)pyrazin-2-yl]-5,6,7,8-tetrahydronaphthalene-2-carboxamide Chemical compound NC1CC=2C=CC(=CC2CC1)C(=O)NC1=CC=C(C=C1)C(F)(F)F.NC1CC=2C=CC(=CC2CC1)C(=O)NC1=NC=C(N=C1)C(F)(F)F VFRZKDPREVZOHV-UHFFFAOYSA-N 0.000 claims 1
- YECPWYJCTUNOCG-ALKXEWLGSA-N FC(C1=CC=C(C=C1)NC=1C=C2CC[C@@H](CC2=CC1)N)(F)F.FC(C=1C=CC(=NC1)NC=1C=C2CC[C@@H](CC2=CC1)N)(F)F Chemical compound FC(C1=CC=C(C=C1)NC=1C=C2CC[C@@H](CC2=CC1)N)(F)F.FC(C=1C=CC(=NC1)NC=1C=C2CC[C@@H](CC2=CC1)N)(F)F YECPWYJCTUNOCG-ALKXEWLGSA-N 0.000 claims 1
- PCULFJNHEYGGBQ-UHFFFAOYSA-N NC1CC=2C=CC(=CC2CC1)C(=O)NC1=CC(=CC=C1)OC.NC1CC=2C=CC(=CC2CC1)C(=O)NC=1C=NC(=CC1)Cl Chemical compound NC1CC=2C=CC(=CC2CC1)C(=O)NC1=CC(=CC=C1)OC.NC1CC=2C=CC(=CC2CC1)C(=O)NC=1C=NC(=CC1)Cl PCULFJNHEYGGBQ-UHFFFAOYSA-N 0.000 claims 1
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- XYVFFEQLUJRKPN-UHFFFAOYSA-N tert-butyl N-[6-[[1-(2,2-difluoroethyl)-5-propylpyrazole-3-carbonyl]amino]-1,2,3,4-tetrahydronaphthalen-2-yl]carbamate Chemical compound FC(CN1N=C(C=C1CCC)C(=O)NC=1C=C2CCC(CC2=CC=1)NC(OC(C)(C)C)=O)F XYVFFEQLUJRKPN-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
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- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
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- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/18—One oxygen or sulfur atom
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- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
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- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
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- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D241/20—Nitrogen atoms
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- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D261/18—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen
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- C—CHEMISTRY; METALLURGY
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- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/58—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
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- C—CHEMISTRY; METALLURGY
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- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
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- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2121/00—Preparations for use in therapy
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
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- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
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- C—CHEMISTRY; METALLURGY
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/10—One of the condensed rings being a six-membered aromatic ring the other ring being six-membered, e.g. tetraline
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EP14179042.8 | 2014-07-30 | ||
EP14179042 | 2014-07-30 | ||
PCT/EP2015/067106 WO2016016162A1 (en) | 2014-07-30 | 2015-07-27 | 6-amino-5,6,7,8-tetrahydronaphthalen-2-yl or 3-aminochroman-7-yl derivatives as taar modulators |
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CN106715395A CN106715395A (zh) | 2017-05-24 |
CN106715395B true CN106715395B (zh) | 2020-05-12 |
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CN201580035425.9A Active CN106715395B (zh) | 2014-07-30 | 2015-07-27 | 作为taar调节剂的6-氨基-5,6,7,8-四氢萘-2-基或3-氨基色满-7-基衍生物 |
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EP (1) | EP3174853B1 (ja) |
JP (1) | JP6383860B2 (ja) |
KR (1) | KR101800594B1 (ja) |
CN (1) | CN106715395B (ja) |
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CA (1) | CA2954088A1 (ja) |
MX (1) | MX2016016606A (ja) |
RU (1) | RU2017103943A (ja) |
TW (2) | TW201617309A (ja) |
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US20190201410A1 (en) * | 2016-06-02 | 2019-07-04 | Purdue Pharma L.P. | Trace amine associated receptor 1 agonists and partial agonists for pain treatment |
CN112370455A (zh) * | 2020-10-19 | 2021-02-19 | 济南大学 | 一种磺酰胺衍生物作为α-葡萄糖苷酶抑制剂及其应用 |
WO2022204150A1 (en) * | 2021-03-22 | 2022-09-29 | Blue Oak Pharmaceuticals, Inc. | Compounds and compositions for treating cns disorders |
Citations (2)
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CN101068801A (zh) * | 2004-10-14 | 2007-11-07 | 艾博特股份有限两合公司 | 适用于治疗对于多巴胺d3受体的调节有反应的疾病的芳基磺酰基甲基或芳基磺酰胺取代的芳族化合物 |
WO2014041007A1 (en) * | 2012-09-14 | 2014-03-20 | F. Hoffmann-La Roche Ag | Pyrazole carboxamide derivatives as taar modulators for use in the treatment of several disorders, such as depression, diabetes and parkinson's disease |
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SI0923542T1 (en) * | 1996-05-31 | 2004-02-29 | Pharmacia & Upjohn Company | Aryl substituted cyclic amines as selective dopamine d3 ligands |
GB9807903D0 (en) * | 1998-04-14 | 1998-06-10 | Smithkline Beecham Plc | Novel compounds |
EP1218336A2 (en) | 1999-09-20 | 2002-07-03 | Takeda Chemical Industries, Ltd. | Melanin concentrating hormone antagonist |
CA2545100A1 (en) * | 2003-11-08 | 2005-05-19 | Bayer Healthcare Ag | Bicyclic amide, carbamate or urea derivatives as vanilloid receptor modulators |
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2015
- 2015-07-27 WO PCT/EP2015/067106 patent/WO2016016162A1/en active Application Filing
- 2015-07-27 CA CA2954088A patent/CA2954088A1/en not_active Abandoned
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- 2015-07-27 TW TW104124294A patent/TW201617309A/zh unknown
- 2015-07-27 CN CN201580035425.9A patent/CN106715395B/zh active Active
- 2015-07-27 KR KR1020177002265A patent/KR101800594B1/ko not_active Expired - Fee Related
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Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101068801A (zh) * | 2004-10-14 | 2007-11-07 | 艾博特股份有限两合公司 | 适用于治疗对于多巴胺d3受体的调节有反应的疾病的芳基磺酰基甲基或芳基磺酰胺取代的芳族化合物 |
WO2014041007A1 (en) * | 2012-09-14 | 2014-03-20 | F. Hoffmann-La Roche Ag | Pyrazole carboxamide derivatives as taar modulators for use in the treatment of several disorders, such as depression, diabetes and parkinson's disease |
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TW201617309A (zh) | 2016-05-16 |
CA2954088A1 (en) | 2016-02-04 |
JP6383860B2 (ja) | 2018-08-29 |
EP3174853B1 (en) | 2018-12-12 |
RU2017103943A3 (ja) | 2018-12-21 |
CN106715395A (zh) | 2017-05-24 |
AR101339A1 (es) | 2016-12-14 |
KR20170020521A (ko) | 2017-02-22 |
KR101800594B1 (ko) | 2017-11-22 |
WO2016016162A1 (en) | 2016-02-04 |
TW201632508A (zh) | 2016-09-16 |
JP2017523194A (ja) | 2017-08-17 |
EP3174853A1 (en) | 2017-06-07 |
MX2016016606A (es) | 2017-04-27 |
US9957261B2 (en) | 2018-05-01 |
US20170137416A1 (en) | 2017-05-18 |
RU2017103943A (ru) | 2018-08-28 |
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